TY - JOUR
T1 - Simultaneous onset of type 1 diabetes mellitus and silent thyroiditis under durvalumab treatment
AU - León Mengíbar, José
AU - Capel, Ismael
AU - Bonfill Abella, Teresa
AU - Mazarico Altisent, Isabel
AU - Casamitjana Espuña, Laia
AU - Caixas Pedragos, Maria Assumpta
AU - Rigla Cros, Maria Mercedes
PY - 2019/7/15
Y1 - 2019/7/15
N2 - SummaryDurvalumab, a human immunoglobulin G1 kappa monoclonal antibody that blocks the interaction of programmed cell death ligand 1 (PD-L1) with the PD-1 and CD80 (B7.1) molecules, is increasingly used in advanced neoplasias. Durvalumab use is associated with increased immune-related adverse events. We report a case of a 55-year-old man who presented to our emergency room with hyperglycaemia after receiving durvalumab for urothelial high-grade non-muscle-invasive bladder cancer. On presentation, he had polyuria, polyphagia, nausea and vomiting, and laboratory test revealed diabetic ketoacidosis (DKA). Other than durvalumab, no precipitating factors were identified. Pre-durvalumab blood glucose was normal. The patient responded to treatment with intravenous fluids, insulin and electrolyte replacement. Simultaneously, he presented a thyroid hormone pattern that evolved in 10 weeks from subclinical hyperthyroidism (initially attributed to iodinated contrast used in a previous computerised tomography) to overt hyperthyroidism and then to severe primary hypothyroidism (TSH: 34.40 µU/mL, free thyroxine (FT4): Learning pointsPatients treated with anti-PD-L1 should be screened for the most common immune-related adverse events (irAEs).
Glucose levels and thyroid function should be monitored before and during the treatment.
Durvalumab is mainly associated with thyroid and endocrine pancreas dysfunction.
In the patients with significant autoimmune background, risk–benefit balance of antineoplastic immunotherapy should be accurately assessed.
AB - SummaryDurvalumab, a human immunoglobulin G1 kappa monoclonal antibody that blocks the interaction of programmed cell death ligand 1 (PD-L1) with the PD-1 and CD80 (B7.1) molecules, is increasingly used in advanced neoplasias. Durvalumab use is associated with increased immune-related adverse events. We report a case of a 55-year-old man who presented to our emergency room with hyperglycaemia after receiving durvalumab for urothelial high-grade non-muscle-invasive bladder cancer. On presentation, he had polyuria, polyphagia, nausea and vomiting, and laboratory test revealed diabetic ketoacidosis (DKA). Other than durvalumab, no precipitating factors were identified. Pre-durvalumab blood glucose was normal. The patient responded to treatment with intravenous fluids, insulin and electrolyte replacement. Simultaneously, he presented a thyroid hormone pattern that evolved in 10 weeks from subclinical hyperthyroidism (initially attributed to iodinated contrast used in a previous computerised tomography) to overt hyperthyroidism and then to severe primary hypothyroidism (TSH: 34.40 µU/mL, free thyroxine (FT4): Learning pointsPatients treated with anti-PD-L1 should be screened for the most common immune-related adverse events (irAEs).
Glucose levels and thyroid function should be monitored before and during the treatment.
Durvalumab is mainly associated with thyroid and endocrine pancreas dysfunction.
In the patients with significant autoimmune background, risk–benefit balance of antineoplastic immunotherapy should be accurately assessed.
UR - https://europepmc.org/articles/PMC8115434
U2 - 10.1530/edm-19-0045
DO - 10.1530/edm-19-0045
M3 - Article
C2 - 31310083
SN - 2052-0573
JO - Endocrinology, diabetes & metabolism case reports
JF - Endocrinology, diabetes & metabolism case reports
ER -